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Journal Abstract Search
162 related items for PubMed ID: 18614259
1. Anti-HIV evaluation of benzo[d]isothiazole hydrazones. Vicini P, Incerti M, La Colla P, Loddo R. Eur J Med Chem; 2009 Apr; 44(4):1801-7. PubMed ID: 18614259 [Abstract] [Full Text] [Related]
2. Synthesis and antiproliferative activity of benzo[d]isothiazole hydrazones. Vicini P, Incerti M, Doytchinova IA, La Colla P, Busonera B, Loddo R. Eur J Med Chem; 2006 May; 41(5):624-32. PubMed ID: 16540208 [Abstract] [Full Text] [Related]
3. Some hydrazones of 2-aroylamino-3-methylbutanohydrazide: synthesis, molecular modeling studies, and identification as stereoselective inhibitors of HIV-1. Tatar E, Küçükgüzel I, Daelemans D, Talele TT, Kaushik-Basu N, De Clercq E, Pannecouque C. Arch Pharm (Weinheim); 2013 Feb; 346(2):140-53. PubMed ID: 23280502 [Abstract] [Full Text] [Related]
4. Synthesis and antiviral evaluation of new N-acylhydrazones containing glycine residue. Tian B, He M, Tan Z, Tang S, Hewlett I, Chen S, Jin Y, Yang M. Chem Biol Drug Des; 2011 Mar; 77(3):189-98. PubMed ID: 21306567 [Abstract] [Full Text] [Related]
5. Structural modifications of DAPY analogues with potent anti-HIV-1 activity. Feng XQ, Liang YH, Zeng ZS, Chen FE, Balzarini J, Pannecouque C, De Clercq E. ChemMedChem; 2009 Feb; 4(2):219-24. PubMed ID: 19090525 [Abstract] [Full Text] [Related]
6. New pyridinone derivatives as potent HIV-1 nonnucleoside reverse transcriptase inhibitors. Le Van K, Cauvin C, de Walque S, Georges B, Boland S, Martinelli V, Demonté D, Durant F, Hevesi L, Van Lint C. J Med Chem; 2009 Jun 25; 52(12):3636-43. PubMed ID: 19469474 [Abstract] [Full Text] [Related]
7. Parallel one-pot synthesis and structure-activity relationship study of symmetric formimidoester disulfides as a novel class of potent non-nucleoside HIV-1 reverse transcriptase inhibitors. Cesarini S, Spallarossa A, Ranise A, Schenone S, Bruno O, La Colla P, Casula L, Collu G, Sanna G, Loddo R. Bioorg Med Chem; 2008 Jun 15; 16(12):6353-63. PubMed ID: 18502646 [Abstract] [Full Text] [Related]
8. Synthesis and anti-HIV-1 activity of new MKC-442 analogues with an alkynyl-substituted 6-benzyl group. Aly YL, Pedersen EB, La Colla P, Loddo R. Arch Pharm (Weinheim); 2007 May 15; 340(5):225-35. PubMed ID: 17464964 [Abstract] [Full Text] [Related]
9. Synthesis and biological evaluation of C-5 methyl substituted 4-arylthio and 4-aryloxy-3-Iodopyridin-2(1H)-one type anti-HIV agents. Guillemont J, Benjahad A, Oumouch S, Decrane L, Palandjian P, Vernier D, Queguiner L, Andries K, de Béthune MP, Hertogs K, Grierson DS, Nguyen CH. J Med Chem; 2009 Dec 10; 52(23):7473-87. PubMed ID: 19645483 [Abstract] [Full Text] [Related]
10. Design, synthesis, and SAR of naphthyl-substituted Diarylpyrimidines as non-nucleoside inhibitors of HIV-1 reverse transcriptase. Liang YH, Feng XQ, Zeng ZS, Chen FE, Balzarini J, Pannecouque C, De Clercq E. ChemMedChem; 2009 Sep 10; 4(9):1537-45. PubMed ID: 19591191 [Abstract] [Full Text] [Related]
11. Synthesis and antiviral activities of novel acylhydrazone derivatives targeting HIV-1 capsid protein. Tian B, He M, Tang S, Hewlett I, Tan Z, Li J, Jin Y, Yang M. Bioorg Med Chem Lett; 2009 Apr 15; 19(8):2162-7. PubMed ID: 19297155 [Abstract] [Full Text] [Related]
12. 2H-Pyrrolo[3,4-b] [1,5]benzothiazepine derivatives as potential inhibitors of HIV-1 reverse transcriptase. Di Santo R, Costi R. Farmaco; 2005 May 15; 60(5):385-92. PubMed ID: 15910811 [Abstract] [Full Text] [Related]
13. Non-nucleoside HIV-1 reverse transcriptase inhibitors. Part 13: synthesis of fluorine-containing diaryltriazine derivatives for in vitro anti-HIV evaluation against wild-type strain. Xiong YZ, Chen FE, Balzarini J, De Clercq E, Pannecouque C. Chem Biodivers; 2009 Apr 15; 6(4):561-8. PubMed ID: 19353537 [Abstract] [Full Text] [Related]
14. Design, synthesis, and evaluation of 2-aryl-3-heteroaryl-1,3-thiazolidin-4-ones as anti-HIV agents. Rawal RK, Tripathi R, Katti SB, Pannecouque C, De Clercq E. Bioorg Med Chem; 2007 Feb 15; 15(4):1725-31. PubMed ID: 17178227 [Abstract] [Full Text] [Related]
15. Novel 1,2,3-thiadiazole derivatives as HIV-1 NNRTIs with improved potency: Synthesis and preliminary SAR studies. Zhan P, Liu X, Li Z, Fang Z, Li Z, Wang D, Pannecouque C, Clercq ED. Bioorg Med Chem; 2009 Aug 15; 17(16):5920-7. PubMed ID: 19620009 [Abstract] [Full Text] [Related]
16. Synthesis and studies of new 2-(coumarin-4-yloxy)-4,6-(substituted)-S-triazine derivatives as potential anti-HIV agents. Mahajan DH, Pannecouque C, De Clercq E, Chikhalia KH. Arch Pharm (Weinheim); 2009 May 15; 342(5):281-90. PubMed ID: 19415671 [Abstract] [Full Text] [Related]
17. Structure-activity relationship in the 3-iodo-4-phenoxypyridinone (IOPY) series: The nature of the C-3 substituent on anti-HIV activity. Benjahad A, Oumouch S, Guillemont J, Pasquier E, Mabire D, Andries K, Nguyen CH, Grierson DS. Bioorg Med Chem Lett; 2007 Feb 01; 17(3):712-6. PubMed ID: 17157017 [Abstract] [Full Text] [Related]
18. 1,2,3-Selenadiazole thioacetanilides: synthesis and anti-HIV activity evaluation. Zhan P, Liu X, Fang Z, Pannecouque C, De Clercq E. Bioorg Med Chem; 2009 Sep 01; 17(17):6374-9. PubMed ID: 19647440 [Abstract] [Full Text] [Related]
19. Solution- and solid-phase synthesis and anti-HIV activity of maslinic acid derivatives containing amino acids and peptides. Parra A, Rivas F, Lopez PE, Garcia-Granados A, Martinez A, Albericio F, Marquez N, Muñoz E. Bioorg Med Chem; 2009 Feb 01; 17(3):1139-45. PubMed ID: 19135380 [Abstract] [Full Text] [Related]
20. Investigation on the role of the tetrazole in the binding of thiotetrazolylacetanilides with HIV-1 wild type and K103N/Y181C double mutant reverse transcriptases. Gagnon A, Landry S, Coulombe R, Jakalian A, Guse I, Thavonekham B, Bonneau PR, Yoakim C, Simoneau B. Bioorg Med Chem Lett; 2009 Feb 15; 19(4):1199-205. PubMed ID: 19138518 [Abstract] [Full Text] [Related] Page: [Next] [New Search]